ENST00000355630.10:c.777+59A>T
MANE Select
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ENSP00000347847.5:n.777+59A>T
|
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ENST00000402042.7:c.777+59A>T
|
ENSP00000385584.3:n.777+59A>T
|
|
ENST00000407029.7:c.477+59A>T
|
ENSP00000385835.1:n.477+59A>T
|
|
ENST00000651595.2:c.777+59A>T
|
ENSP00000498277.2:n.777+59A>T
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ENST00000652095.2:c.582+59A>T
|
ENSP00000498671.1:n.582+59A>T
|
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ENST00000355630.7:c.477+59A>T
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ENSP00000347847.3:n.477+59A>T
|
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ENST00000396617.7:c.477+59A>T
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ENSP00000379861.3:n.477+59A>T
|
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ENST00000402042.5:c.477+59A>T
|
ENSP00000385584.1:n.477+59A>T
|
|
ENST00000407029.5:c.477+59A>T
|
ENSP00000385835.1:n.477+59A>T
|
|
ENST00000614754.4:c.480+59A>T
|
ENSP00000484786.1:n.480+59A>T
|
|
ENST00000618196.4:c.582+59A>T
|
ENSP00000479510.1:n.582+59A>T
|
|
ENST00000618417.1:c.-1245-11255A>T
|
ENSP00000484628.1:n.-1245-11255A>T
|
|
ENST00000620651.4:c.480+59A>T
|
ENSP00000478420.1:n.480+59A>T
|
|
NM_001282660.1:c.477+59A>T
|
NP_001269589.1:n.477+59A>T
|
|
NM_001282661.1:c.477+59A>T
|
NP_001269590.1:n.477+59A>T
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NM_001282662.1:c.477+59A>T
|
NP_001269591.1:n.477+59A>T
|
|
NM_020831.4:c.477+59A>T
|
NP_065882.1:n.477+59A>T
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|
XM_005261691.3:c.582+59A>T
|
XP_005261748.1:n.582+59A>T
|
|
XM_005261692.1:c.558+59A>T
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XP_005261749.1:n.558+59A>T
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XM_005261694.1:c.477+59A>T
|
XP_005261751.1:n.477+59A>T
|
|
XM_011530283.1:c.558+59A>T
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XP_011528585.1:n.558+59A>T
|
|
XM_011530284.1:c.582+59A>T
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XP_011528586.1:n.582+59A>T
|
|
XM_011530285.1:c.354+59A>T
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XP_011528587.1:n.354+59A>T
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|
XM_011530286.1:c.354+59A>T
|
XP_011528588.1:n.354+59A>T
|
|
XM_011530287.1:c.-18-462A>T
|
XP_011528589.1:n.-18-462A>T
|
|
NM_001282661.2:c.777+59A>T
|
NP_001269590.2:n.777+59A>T
|
|
NM_001282662.2:c.777+59A>T
|
NP_001269591.2:n.777+59A>T
|
|
NM_001318139.1:c.582+59A>T
|
NP_001305068.1:n.582+59A>T
|
|
NM_020831.5:c.777+59A>T
|
NP_065882.2:n.777+59A>T
|
|
XM_017028888.2:c.558+59A>T
|
XP_016884377.1:n.558+59A>T
|
|
XM_017028889.1:c.354+59A>T
|
XP_016884378.1:n.354+59A>T
|
|
NM_001282660.2:c.477+59A>T
|
NP_001269589.1:n.477+59A>T
|
|
NM_001282661.3:c.777+59A>T
|
NP_001269590.2:n.777+59A>T
|
|
NM_001282662.3:c.777+59A>T
|
NP_001269591.2:n.777+59A>T
|
|
NM_001318139.2:c.582+59A>T
|
NP_001305068.1:n.582+59A>T
|
|
NM_020831.6:c.777+59A>T
MANE Select
|
NP_065882.2:n.777+59A>T
|
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